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rs987106

From SNPedia

Orientationminus
Stabilizedminus
Make rs987106(A;A)
Make rs987106(A;T)
Make rs987106(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position35875491
GeneIL7R
is asnp
is mentioned by
dbSNPrs987106
ebirs987106
HLIrs987106
Exacrs987106
Varsomers987106
Maprs987106
PheGenIrs987106
hapmaprs987106
1000 genomesrs987106
hgdprs987106
ensemblrs987106
gopubmedrs987106
geneviewrs987106
scholarrs987106
googlers987106
pharmgkbrs987106
gwascentralrs987106
openSNPrs987106
23andMers987106
23andMe allrs987106
SNP Nexus

SNPshotrs987106
SNPdbers987106
MSV3drs987106
GWAS Ctlgrs987106
GMAF0.4601
Max Magnitude
? (A;A) (A;T) (T;T) 28
Rs987106
PubMed [PMID 17660816]
Affy Probeset SNP_A-4264835
Affy Orientation same
On GW 5.0 1
Alleles A/B A/T
Ancestral T
Population
Allele T
Case Freq.
Control Freq.
Odds Ratio Het 0.79
Odds Ratio Hom 1.26
Odds Ratio All
Disease Multiple sclerosis (MS)


Neighborrs3194051
Distance681

rs987106 increases susceptibility to Multiple sclerosis 0.79 times for heterozygotes (AT) and 1.26 times for homozygotes (TT) [PMID 17660816]




[PMID 22329520] Identification of IL7RA risk alleles for rapid progression during HIV-1 infection: a comprehensive study in the GRIV cohort

[PMID 18563381] Study of the association between the CAPSL-IL7R locus and type 1 diabetes.


GET Evidence
rs987106
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.543224
summary